A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18188835



Internal ID20755875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:13353595..13476784hg38UCSC Ensembl
chr17:13256912..13380101hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38123190
hg19123190
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6513388
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18188835
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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